Actively Recruiting
M2VA Pain Care Pathway
Led by Yale University · Updated on 2025-11-05
1800
Participants Needed
1
Research Sites
197 weeks
Total Duration
On this page
Sponsors
Y
Yale University
Lead Sponsor
N
National Center for Complementary and Integrative Health (NCCIH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this 2-cohort, cluster randomized, type 2 hybrid trial is to test the effectiveness, cost-effectiveness and patient-level effects of an implementation facilitation strategy in helping M2VA case managers adopt a Military2VA Pain Care Pathway (M2VAPCP) intervention. The main questions it aims to answer are: Will adding implementation facilitation to training-as-usual for M2VAPCP result in a higher proportion of Veterans who receive M2VAPCP compared to training-as-usual alone? Will adding implementation facilitation to training-as-usual for M2VAPCP result in better adherence to the M2VAPCP protocol compared to training-as-usual alone? Will implementation facilitation improve Veterans' clinical outcomes (pain, risky substance use) and increase the number of non-pharmacological pain treatments used compared to training-as-usual alone?
CONDITIONS
Official Title
M2VA Pain Care Pathway
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Enrollment within one year of ending military service
- Filed a service-connection claim for a musculoskeletal disorder (back, neck, knee, or shoulder condition)
- Lives within the catchment area of a participating site
You will not qualify if you...
- Unable to complete study assessments due to incapacity, incarceration, or other reasons
- Does not have a landline or cell phone to complete study assessments
- Unable to provide informed consent
- Still on active duty
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
VA Connecticut Healthcare System (VACHS)
West Haven, Connecticut, United States, 06516
Actively Recruiting
Research Team
C
Christina Lazar, MPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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